天境生涯

作为一家年轻的生物技术公司。我们相信团队精神中“秉承完美、追求创新、不断进取”是获得成功至关重要的原因,也是我们企业的进步核心。天境生物在高速发展的同时,更致力于为我们的员工提供丰富的职业发展平台,以此拓展员工的个人潜力,帮助他们实现自己的梦想。

加入我们

我们致力于为全球的患者带来创新的治疗方法。如果您有和我们一样的激情和梦想,欢迎加入天境大家庭,投入改善患者生存质量的新旅程。

如果您对天境职位感兴趣,请将您的简历发送至:

hrdept@i-mabbiopharma.com
(Associate/ Sr.) Clinical Research Manager
SH/BJ
R&D
Direct Report 直线经理:临床研究(副)总监
Direct Subordinates 直接下属:(高级)临床监查员
Primary Function 主要职能:
负责临床监查员人员管理,确保临床研究合适的人员分配,确保CRA获得履行自职责所需的技能。

Major Responsibilities and Duties 主要职责和任务 :
  根据公司的政策和相关法规管理员工。职责包括规划、分配和指导工作;评估绩效和指导职业发展;奖励和惩罚员工;员工工作关系问题的处理和解决。人力资源相关事项的审批。
  参与员工招聘和选拔过程。新员工入职培训相关事宜的管理。
  确保员工有适当的材料、系统权限和培训,以完成其工作职责。
  为临床研究项目分配人员,确保被分配人员的经验和培训与临床研究项目匹配。
  定期考察和评估员工的工作,管理员工的工作质量。
  识别质量风险和问题,制定适当的整改措施,预防或纠正员工绩效方面的问题。
  定期审查以确保员工达到规定的工作量、质量和其他指标。
  参与公司或部门的质量或流程改进计划。

Qualifications 资格要求:
  大学本科及以上学历。
  临床医学、药学、生物学或相关专业。
  至少 5 年临床研究相关经验,其中至少 2 年人员管理经理或相关工作经验。
  熟悉中国药监法规和临床试验要求。
  优秀的领导力。
  有效的沟通和表达技巧。
  优秀的组织和解决问题的能力。
  有效的时间管理技能。
  优秀的中英文书面和口头表达能力。
Send your resume
Regulatory CMC AD/D
SH
R&D
Direct Report 直线经理:VP, RA

Primary Function 主要职能:
• Provide Regulatory CMC leadership within RA and on cross-functional CMC teams
• Maintain up-to-date knowledge and expertise of relevant regulatory authorities and ICH guidelines
• Facilitate timely regulatory approvals of new drugs and life cycle activities by ensuring the quality and appropriateness of submission documents, and maintaining regulatory compliance for investigational and marketed products

Major Responsibilities and Duties 主要职责和任务 :
• Manage project planning, operation and reporting of assigned projects.
• Prepare, review Chemistry, Manufacturing and Controls (CMC) documents for IND/BLA/NDA and their amendments/supplements to assure compliance with regulatory agencies’ requirements and industry standards.
• Develop regulatory CMC strategy and identify key issues throughout the project.
• Evaluate manufacturing change controls, assess regulatory impact, and support their implementation.
• Support QC testing for investigational and commercialized drugs.
• Support GMP site inspection when required by regulatory agency.

Qualifications 资格要求:
• Experience or understanding of drug development process.
• Strong organization, communication, and interpersonal skills is a must
• Knowledge of CMC regulation is a plus
• Excellent time management
• Capability to multi-task and meet challenging timelines
• Chinese writing skills
Send your resume
Medical Writing
SH/BJ
R&D
Direct Report 直线经理:VP, Head of Medical Office
Primary Function 主要职能:
Medical Writer, working closely with I-Mab project team, provides high quality medical writing support to clinical regulatory documents (generally protocols/amendments, Investigator’s Brochures/updates, clinical study reports, safety reports and regulatory authority response documents) across product
development stages.
In addition, Medical Writer is responsible for overseeing medical writing services outsourced to CROs to ensure quality and timely delivery.

Major Responsibilities and Duties 主要职责和任务 :
• Actively participate in project team meetings in the development of clinical documents
• Collaborate with study physician, clinical PM, regulatory team to prepare, consolidate review comments, update and finalize protocol, ICF including any amendment, IB development and update, writing support to support authority responses etc.
• Collaborate with biostatisticians, clinical colleagues to interpret study results and ensure timely and accurate integration of data presented in the statistical tables and listings and other information sources into the CSR
• Ensure all medical writing deliverables prepared per ICH and other relevant regulatory guidelines• Ensure that appropriate quality control (QC) checks are performed on protocol, IB, CSRs, other documents and other medical writing deliverables, as required
• Ensure documents are generated in accordance with agreed internal processes and standards, are submission ready and appropriately stored in an agreed document management system
• Provide thorough and critical review or peer QC support of documents prepared by others, as needed

Qualifications 资格要求:
1. Master’s degree from Chinese universities or bachelor's degree from overseas universities
2. Major in clinical medicine, pharmacy, biology or other related fields
3. 10 years pharmaceutical industry experience with at least 5 years in medical writing
4. Excellent English, both written and spoken
5. Demonstrated ability to communicate clinical data succinctly, clearly and accurately in writing
6. Knowledge of ICH guidelines and regulatory requirements and demonstrated ability to interpret and apply these guidelines in a report writing setting
7. Competence in the use of relevant software applications (e.g., Microsoft Office), templates and other electronic formats
8. Experience of working with electronic document management systems
Send your resume
Clinical Pharmacology Scientist
SH
R&D
Department 部门:免疫和早期研发部,研发部
Direct Report 直线经理:PV&QA Head
Primary Function 主要职能:
临床药剂师确保临床药代动力学(PK),药效动力学(PD),建模和仿真(MS)原理策略的应用有助于提高药物研发效率,对研发药物的 PK/PD 策略负责,向其他战略业务部门、内部和外部相关关键部门提供 PK/PD 策略指导,并提供质量服务。

Major Responsibilities and Duties 主要职责和任务:
• 为多个综合发展项目提供临床 PK/PD 数据分析。
• 与临床团队共同设计多项临床研究中的重要 PK/PD 元素,如首次人体试验,生物等效性,不同药物之间的互做等研究
• 为相关文件提供临床 PK/PD 数据
• 设计、分析、报告和展示 PK/PD 的 MS 计划,包括各个研究阶段的人体 PK/PD 分析
• 审阅相关临床科学文件,包括临床试验方案,SOP,统计分析计划和临床研究报告
• 始终深入掌握药理学,生物学,治疗学,药物代谢,生物分析和生物药剂学知识
• 与内部和外部的相关部门及科学家建立和维持良好的关系
• 维持积极的,结果导向的工作环境,建立伙伴关系和团队合作模型,建立开放,平衡和客观的团队沟通方式
• 审阅或撰写科学出版物,摘要和海报
• 参与业务发展活动,药物评价项目等

Qualifications 资格要求:
• 渊博的 PK/PD 知识
• 具有设计和实施基于模型的药物发展策略的经验
• 具有药物测量学方法论知识
• 熟练应用药代动力学模型软件如 Phoenix WinNonlin
• 最好有熟练使用其他软件如 NONMEM, GastroPlus 和 R 的经验
• 优秀的人际交往能力
• 优秀的临床/科学协作技巧
• 客户导向的工作方式
• 灵活处理相应的工作任务和学习新知识
• 管理多项任务的能力
• 适应复杂的工作环境,重视并促进团队合作
• 至少 3-5 年药物研发工作经验
• 优秀的英文书写和口语能力
• 具有高级学位(理学/药学硕士,理学/药学博士)和/或相关经验 
Send your resume
Senior Scientist
SH
R&D
Direct Report 直线经理:Associate Director
Primary Function 主要职能:
The translational research group leads translational research, biomarker identification and novel targets exploration for I-Mab’s immunology and oncology pipelines.
We are looking for a highly talented and motivated bioinformatics scientist to support biomarker discovery and validation.

Major Responsibilities and Duties 主要职责和任务 :
• Analyzing and interpreting high-throughput genomic and biomedical data
• Designing, developing and deploying robust workflows to analyze high-throughput data, with emphasis on RNA-Seq/ExomeSeq /Panel Sequencing to explore drug target biology.
• Mining proprietary and public biological data/database (TCGA etc) `to generate novel hypotheses or insights
• Building and managing biological database (NGS data etc).
• Presenting analysis results in a clear and concise manner
• Collaborate closely and effectively as a member of global biomarker and translational research team, follow sound scientific practices and maintain effective documentation of activities and analyses.

Qualifications 资格要求:
• PhD degree in bioinformatics / computational biology / genomics related fields; or Master degree with 3 years working experience in the bioinformatics related fields
• Strong programming and scripting abilities in R, and proficient in at least one other programming language (Python, Perl, Shell scripting, Java etc.)
• Comfortably working with Linux system and server/cloud computing environmentJob Descriptions
• Excellent background in analyzing high throughput biomedical data (RNASeq, ExomeSeq and Panel sequencing): data cleaning, functional annotation, normalization, analysis, interpretation and visualization
• Strong statistics and math background
• Familiarity with public databases and tools: NCBI, Ensembl, TCGA, cBioPortal, Oncomine, dbSNP etc
• Experience in database design, analysis pipeline and Rshiny development
• Experience with open-source bioinformatics tools and packages (Bioconductor etc.)
• Self-motivated and enjoys teamworking within an international team and dynamic environment always with timeline in mind
• Thorough understanding and interest in tumor biology and immunology
• Fast learner and excited for new challenges
Send your resume
Team Coordinator
SH
R&D
Direct Report 直线经理:EA, R&D

Primary Function 主要职能:
• Daily admin support
• Ad-hoc tasks supporting to R&D leaders
• Team meetings/events support

Major Responsibilities and Duties 主要职责和任务:
• Daily admin support
• Booking and coordination of meetings
• Expense reimbursement and other business administration
• Ad-hoc tasks supporting to R&D leaders
• Team meetings/events support
• Contact window with external vendors and internal stakeholders such as procurement, finance, etc.

Qualifications 资格要求:
• Bachelor’s degree
• Ability to quickly learn new tools and technologies
• Good interpersonal skills to communicate across functions/departments and the ability to build relationships
• Good written and oral English
• Excellent computer skills like MS Office
• Great attitude under pressure
Send your resume
DM Manager/Sr. Manager
SH
R&D
Primary Function 主要职能:
1) 执行临床数据管理的策略为临床试验的探究和分析提供高质量、有价值和及时的数据以驱动产品线的决策。
2) 协助临床数据管理副总监优化部门的流程和平台以高效地满足公司发展的需要。

Major Responsibilities and Duties 主要职责和任务 :
1) 针对不同复杂程度的临床试验项目,对提供数据管理服务的 CRO 进行监督,承担项目层面数据质量的最终责任。
2) 与临床数据管理团队的成员以及其他临床部门合作建立和完善天境的数据收集和核查的标准。
3) 提供强有力的技术支持以提高临床试验各阶段数据质控的工作效率。
4) 就项目流程或者技术解决方案给出推荐和影响决策。
5) 维护一个积极的、指向结果的工作环境,与其他职能部门建立良好的工作关系,与 CRO 和项目成员建立一个开放、和谐和客观的沟通环境。

Qualifications 资格要求:
1) 生命科学或者相关学科学士以上学位
2) 至少 5 年临床数据管理及其相关的工作经验
3) 有 Medidata Rave 建库经验优先
4) 有基本的编程能力优先
5) 理解临床数据管理系统的设计、开发、验证以及系统交互
6) 良好的沟通和人际能力
Send your resume
(Sr.) CRA
SH/BJ
R&D
Primary Function:
Support (Sr.) Project manager / (Asso.) Project Management Director on Clinical projects to sets up, monitor and report in accordance with ICH/GCP, the company's requirements and the local/regional regulation to achieve clinical operation and study target on timeline, quality and cost

Major Responsibilities and Duties:
1. Participates in the development of clinical trial documents in collaboration with the project manager.
2. Identifies and selects investigators/sites in collaboration with the project manager
3. Prepares / collects all documents needed prior to study initiation.
4. Performs study feasibility visits in the investigational sites
5. Organizes / participates in study site initiation visit in which are provided scientific and technical knowledge concerning the study procedures and its organisation.
6. Ensures monitoring follow up:
• Maintain the relationship with the investigational site
• Follow up of trial progress and quality control of data (source document check)
• Documentation of protocol violations, adverse events and premature treatment cessation.
• Identification and resolution of all problems: logistical, methodological, human technical, which occur during the trial.
• Management of the local trial files
• Management of the investigator’s trial file
• Management of trial related logistics
• Detection and reporting of deviations, finding and implementing corrective measures
7. Provides timely monitoring reports for all visits / contacts in appropriate reports.
8. Performs study close out visits to close investigational site.
9. Prepares, organizes and participates in investigator’s meetings
10. Manage study TMF filing and archiving
11. Participates in internal & external education and training

Qualifications:
1. Bachelor’s degree and above
2. Major in clinical medicine, pharmacy and biology or relevant;
3. Have 2 years of relevant monitoring experience in clinical trial, and have knowledge reserve of clinical trial management specification (GCP)
4. Strong communication and coordination skills with internal /external clients
5. strong team spirit, sense of responsibility, proactive, careful and meticulous
6. Good computer skills, including proficiency in Microsoft Word, Excel and PowerPoint.
7. Good oral and written communication skills.
8. Good organization and problem-solving skills
9. Have a talent with effective time management.
Send your resume
PML(Sr. ) Manager
SH
R&D
Title 职位:PMO Operation (Sr.) Manager
Starting Date 任职时间:Jul. 2020
Direct Report 直线经理:Danqing Xu

Primary Function 主要职能:
The PMO operation manager (POM) will provide strong support to Program Management Leaders (PML) in terms of backend project management database maintenance, sharepoint site maintenance and project finance integrative maintenance.
In this position of technical subject of matters, PMO operation manager will work as Center of Excellence to create workflow and process with PMLs to ensure the execution of product strategy with concomitant goals and objectives in an alignment with I-Mab vision.

Major Responsibilities and Duties 主要职责和任务 :
•Be responsible for daily Sharepoint site architecture and maintenance;
•Work with PMLs (Program Management Lead) to govern projects progress tracking (milestones record, project team structure et al);
•Responsible for PMO workflow and process (time reporting, budget planning, portfolio review et al), work with IT and finance partners to optimize project related process;
•Create and maintain project related template files;
•Responsible for maintaining Project Management System.

Qualifications 资格要求:
• Medical, life sciences or business management related degree is required; Project management related training and understanding of PM related core activity is preferred;
• 3-5 years of pharmaceutical industry experience is required; experiences in pharma R&D organization is a plus;
• Skills in MS office (sharepoint, onenote and MS 365 environment included) is a must.Analytical, synthesis and reporting skills is preferred;
• The ability to work with cross-functional teams in a matrix environment is a must;
• Demonstrated ability to create organized workflow/process and resolve problems from multiple clues is required.
Send your resume
Formulation Development, Director
SH
CMC
Primary Function 主要职能:
The Director, Formulation Development will be responsible for leading formulation development of biologics. This individual will lead phase appropriate formulation and drug product process development for biologics programs to advance the portfolio. This position will work collaboratively with the various
functional areas within process and CDMOs. This role will be a key contributor within the CMC organization at I-Mab. The successful candidate will be a formulation specialist with a proven track record in managing and leading biologic formulations.

Major Responsibilities and Duties 主要职责和任务 :
1. Lead the development of formulation strategies in the design and implementation of stable formulations of monoclonal antibodies;
2. Provide technical and scientific direction to CDMOs and external laboratories to ensure project deadlines and performance standards are met;
3. Lead the development/optimization of scalable, efficient, and cost-effective formulation efforts;
4. Responsible for technical leadership in technical issue resolution with CDMO partners,including design of experiments and interpretation of results;
5. Oversee the preparation of technical reports, data summaries and CMC related documents required for various regulatory submissions;
6. Oversee the development of technical transfer protocols and supervise the transfer of drug product manufacturing processes into cGMP drug product manufacturing facilities;
7. Review analytical and clinical data to make scientific conclusions;
8. Create and review technical documents, reports, and presentations for cross functional teams;
9. Manage SOPs, change controls, deviations and CAPAs with thorough knowledge of Good Manufacturing Practices.

Qualifications 资格要求:
1. Masters or PhD (preferred) in pharmaceutical sciences, biochemistry or another relevant field;
2. Eight-plus years of relevant biopharmaceutical industry experience with experience in formulation of biologics;
3. Demonstrated ability to successfully work with and influence contract manufacturing partners while maintaining a positive working relationship;
4. Proven leadership in developing new formulations/processes and scaling them up for implementation;
5. Ability to work/lead in a dynamic group that takes a multi-disciplined team approach to executing and achieving departmental and corporate goals;
6. Demonstrated communication, problem-solving, leadership, and negotiation/decision-making skills;
7. Desire to work in a fast-paced, innovative environment;
8. Natural collaborator who enjoys working on a cross-functional team.
Send your resume
Senior Manager/ Associate Director/ Director of CMC RA
SH
CMC
Direct Report 直线经理:Jack Qin

Primary Function 主要职能:
The purpose of this position is to play a leading role managing and executing CMC regulatory strategies,and ensure product development and manufacturing in compliance with relevant regulations, guidelines,and industry standards.This position requires extensive knowledge of biologics CMC Regulatory and CMC lifecycle management. Substantial experience with IND/BLA authorship and submissions.

Major Responsibilities and Duties 主要职责和任务 :
• Provide CMC regulatory leadership for Global development and registration programs (e.g., INDs,BLAs and Variations) in China.
• Research and interpret China and global CMC regulations and provide strategic direction and regulatory guidance to Quality, Manufacturing, Process Development as well as partners and CDMOs.
• Lead authoring and review of IND/BLA filing documents and promote product development in alignment with China and global CMC regulatory requirements for clinical development, registration as well as lifecycle biologic products.
• Collaborate with Quality teams in compliance audits at CDMOs and Vendors; Assist in PAIs and other inspections in manufacturing, QC labs and supply chain.

Qualifications 资格要求:
1. Ph.D/MS in life sciences with minimal 10 years’ experience in the biopharmaceutical industry;
2. Previous working experience in Biologics Process Development, GMP manufacturing or Quality desired;
3. Extensive experience in preparation of IND/BLA filings, and Variations for biologic products, and interactions with Health Authorities in China. The experience of US IND/ BLA is plus. 
Send your resume
药学工艺开发/项目管理 高级总监/总监/经理
SH
药学工艺开发部
Direct Report 直线经理:药学工艺开发部负责人
Primary Function 主要职能:领导和管理天境生物的工艺开发团队/小组,负责单抗类产品的工艺开发,或外包项目管理,或工艺技术转移、或实验室的工艺平台搭建

Major Responsibilities and Duties 主要职责和任务 :
• 负责单抗类新产品的工艺开发,技术转移,中试放大的计划和策略,管理 CMC 开发的整个流程及执行项目,
• 技术支持和推进公司内部生产及外包的 CMC 项目,协调公司内外资源
• 负责工艺开发实验室的建立,工艺开发技术平台的搭建。
• 按照 CMC 开发的相关国内外要求,组织撰写 IND 有关申报资料,回答监管机构审计和审评等方面的问题。

Qualifications 资格要求:
• 具有化学工程,药学或生命科学相关的硕士或博士学位
• 需有工艺开发相关 5 年以上的经验,熟悉整个单抗类分子新药产品工艺开发的流程,如有细胞株构建,细胞培养、纯化,制剂或分析方面等方面的经验优先。
• 了解 FDA,NMPA/CDE 新药开发的法规
• 有过和 CMO 或 CRO 开发 CMC 项目管理和合作经验,
• 具备良好的执行,团队建设,人际沟通和组织协调能力,
• 有海外制药公司或跨国公司工作经验的,具备良好英文沟通能力为优先
• 有 cGMP 经验为优先
Send your resume
BD Head
SH
Commercial
Direct Report 直线经理:Chief Commercial Officer
Primary Function 主要职能:业务拓展

Major Responsibilities and Duties 主要职责和任务 :
1. 根据公司战略定位,寻访目标客户并进行商务谈判,引进新产品,编写可行性报告;
2. 建立系统的新业务拓展渠道,发现新的业务类型、新的合作伙伴、新市场机会,对公司进行新业务拓展;
3. 确定意向客户,建立商业合作关系,洽谈、促进项目合作达成;
4. 制订新产品相应市场推广策略。

Qualifications 资格要求:
1. 医药或生命科学相关专业,博士学历优先;
2. 医药行业背景,10 年以上 BD 经验,有肿瘤项目经验优先(大/小分子皆可);
3. 英文听说读写流利;
4. 具备丰富的并购项目、late stage 项目引进的经验;
5. 掌握国内外医药市场信息获取渠道和调研立项分析方法;
6. 熟悉医药营销、药品研发、市场调查,了解药品报批、临床试验、药品专利分析等相关工作;
7. 熟悉各大类产品线主要产品,明确制药行业的现状和发展趋势,在医药行业有丰富的人脉资源优先;
8. 优秀的商务谈判能力、项目管理能力、团队管理能力,能适应经常短期出差。 
Send your resume
Director/Manager of Global Business Development
SH
GBD
Direct Report 直线经理:Senior Director of Global Business Development
Primary Function 主要职能:
Asia focused Search & Evaluation
Deal valuation
Business Execution
Major Responsibilities and Duties 主要职责和任务 :
▪ Work closely with Senior Director of Global Business Development, to drive the overall business development activities at I-MAB
▪ Identify and build relationships with Asia based biopharmaceutical industry companiesand identify potential business opportunities, follow through in negotiating and driving partnering efforts to the completion of successful partnership agreements
▪ Communicate effectively with IMAB executives and stake holders in identifying value add opportunities negotiating, and completing contract agreements that form the basis for long term strategic partnerships
▪ Understand and know how to navigate Asia biopharmaceutical market, including investment opportunities, products,
▪ Effectively collaborate with internal departments (Discovery, Medical, ClinicalDevelopment, RA) throughout the process of establishing and executing key
partnerships
▪ Maintain key external relationships while identifying new potential partners within the areas you have been assigned
▪ Possess a strong understanding of I-MAB biopharmaceutical products, our key competitors, and how we will position ourselves to success through licensing out and co-development activities
▪ Track and communicate ongoing industry developments to the internal team members and stay up to date on the completive environment

Qualifications 资格要求:
▪ MBA or master’s degree in science or Business,PhD degree preferred
▪ Fluent English speaking, reading, and writing skills
▪ Three years proven track record in biopharmaceutical business development or related markets
▪ Excellent organizational skills, with emphasis on prioritization and goal setting
▪ Superior presentation and communication skills, both written and verbal
▪ Technical skills required to understand, present, and propose biopharmaceutical partnering opportunities both internally as well as to customers
▪ Ability to communicate information, whether technical or non-technical to staff members and customers, in a clear and concise manner
Send your resume
IP Head
SH
法务部
Direct Report:Legal Head

Major Responsibilities and Duties:
1) 公司自有专利的日常维护和管理,包括但不限于与公司内部专利发明人、外部专利申请代理人的沟通协调,撰写专利申请技术交底书,专利申请文件及进度跟踪汇报,专利年费的缴纳和代理费用支付;
2) 被许可专利的维护;
3) 对外许可项目专利尽调等工作支持;
4) 对公司所遇到的纠纷提供专利支持;
5) 与外部专利律师一起梳理建立公司专利管理制度和策略,识别专利管理制度中存在的风险并提出解决方案,协助更新专利管理制度;
6) 积极主动完成上级交办的其他各项专利工作。

Qualifications:
1) 生物医药相关专业硕士及以上学历;
2) 具备专利代理人职业资格证书,具有 5 年及以上专利代理人工作经验以及 5 年以上的涉外专利岗位相关工作经验者或者8 年以上的涉外专利管理岗位工作经验;
3) 具有优秀的专利代理实务和专中英文利文书写作能力,具有较强的分析、判断和解决问题的能力;
4) 具有良好的中英文语言表达及沟通协调能力,能清晰表达专业意见,善于开展跨部门沟通;
5) 具备良好的职业操守及严谨的工作态度,有团队合作精神,能承受一定的工作压力。
Send your resume
Legal Manager
SH
法务部
Title:法务经理
Direct Report:法务副总监

Major Responsibilities and Duties:
1) 对公司日常经营中涉及的法律文件(包括但不限于中英文合同、规章制度等)进行起草、审核、修订和参与谈判;
2) 收集、整理和更新与公司业务相关的中英文合同模板;
3) 对公司合同管理制度进行梳理,识别现有合同管理制度中存在的风险并提出解决方案,协助起草、制定合同管理制
度;
4) 分析公司业务运营可能涉及的法律风险并提出相应的解决方案;
5) 对公司所遇到的纠纷提供法律支持;
6)积极主动完成上级交办的其他各项法务工作。

Qualifications:
1) 全日制法律专业硕士或及以上学历,具有英语国家留学背景者优先;
2) 具有 5 年及以上涉外法律工作经验,具备法律职业资格证书优先;
3) 具有国际律师事务所工作经验、外企法务、非外资企业涉外法务岗位相关工作经验者优先;
4) 具有较好的法学理论功底和法律文书写作能力,具有较强的分析、判断和解决问题的能力;
5) 具备优秀的沟通协调能力,能清晰表达专业法律意见,善于开展跨部门沟通;
6) 具备良好的职业操守及严谨的工作态度,能承受一定的工作压力;
7) 理解能力强,具有良好的中英文语言表达、法律文书撰写及沟通能力,性格开朗大方、接人待物稳重;
8)具有良好的职业道德,有团队合作精神,有责任心。 
Send your resume
版权所有 天境生物科技(上海)有限公司. All rights reserved 2019 沪ICP备17007960号-2